HGVS | Genome Assembly |
---|---|
NC_000008.11:g.23212105T= , CM000670.2:g.23212105T= | GRCh38 |
NC_000008.10:g.23069618T= , CM000670.1:g.23069618T= | GRCh37 |
NC_000008.9:g.23125563T= | NCBI36 |
NG_032107.1:g.18063A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000221132.8:c.403+11A= MANE Select | ENSP00000221132.3:n.403+11A= | |
ENST00000221132.7:c.403+11A= | ENSP00000221132.3:n.403+11A= | |
ENST00000524158.5:c.-204+11A= | ENSP00000428884.1:n.-204+11A= | |
ENST00000613472.1:c.32-9446A= | ENSP00000480778.1:n.32-9446A= | |
NM_003844.3:c.403+11A= | NP_003835.3:n.403+11A= | |
NM_003844.4:c.403+11A= MANE Select | NP_003835.3:n.403+11A= |